Intracytoplasmic sperm injection (ICSI) is an IVF procedure in which a single sperm selected under a microscope is injected directly into the egg. A tiny needle, called a micropipette, is used to perform this delicate procedure. In our practice, ICSI is the routine procedure:
Intracytoplasmic Morphologically Selected Moving Sperm Injection (IMSI) is the preferred method in cases with severe disfigurement in sperm. The most important advantage of this technique is using significantly higher microscopic magnification (more than x6000 times) to select the best sperm cells. This prevents the use of abnormally structured sperm that can negatively affect the fertilization process.
Cases, when no sperm cells are detected in a semen sample, are known as azoospermia. To simplify, we can divide azoospermia cases into two groups.
Several types of operations allow us to find sperm in cases when no sperm is found in the semen sample. The most frequently used operations are:
Once the sperm is received, the sperm cells are treated by embryologists and injected into women's eggs using the ICSI microinjection method. If a good-quality embryo develops, we transfer the embryos into the uterus and wait for the implantation.
Egg freezing is a method of preserving a woman's eggs (oocytes) so she can try and have children at a later date. It’s important to understand that freezing the eggs does not guarantee a future pregnancy. Egg freezing treatment may be recommended to two main groups:
1. Medically necessary:
2. Elective:
Preimplantation genetic testing allows us to examine the chromosomes of embryos obtained through IVF before transferring them back into the maternal womb. Embryos obtained through IVF treatment are expected to reach the blastocyst stage on day 5 or 6. Thanks to the development of science and technologies embryologists using special tools can now safely biopsy embryos that developed to this stage and have a good exterior appearance, after this biopsy embryos are frozen. Laboratory equipment and embryologists’ experience are crucial at this stage. Cells obtained during the biopsy are then sent to the genetics laboratory. Genetic sequencing of embryos is reported back by the laboratory between 10 and 15 days later. Embryo, which is confirmed to be genetically normal, is transferred into the womb in the following months. We may recommend this method to:
The main purpose of preimplantation genetic testing is to study the chromosome structure of the embryos, where normal would be 22 pairs of autosomes (body chromosomes) and 1 pair of allosomes (sex chromosomes: XX for females and XY for males). These pairs of chromosomes must be sequenced in order. Faulty sequencing leads to abnormalities, for example, a chromosome pair having a deficiency on one side (monosomy), or excess on one side (trisomy). The most common known chromosome disorder is 21, or Down Syndrome which is characterized by having 3 chromosomes.
This method enables chromosomally normal embryos to be selected for transfer back to the mother. Moreover, this method allows couples with familial hereditary genetic diseases to have healthy babies.
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